A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432539



Internal ID21090092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32119345..32119715hg38UCSC Ensembl
chr8:31976861..31977231hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168201
Samples
Known GenesNRG1, NRG1-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432539
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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